222 related articles for article (PubMed ID: 11775055)
1. Tyrp1 and oculocutaneous albinism type 3.
Sarangarajan R; Boissy RE
Pigment Cell Res; 2001 Dec; 14(6):437-44. PubMed ID: 11775055
[TBL] [Abstract][Full Text] [Related]
2. Mutant alleles at the brown locus encoding tyrosinase-related protein-1 (TRP-1) affect proliferation of mouse melanocytes in culture.
Sarangarajan R; Zhao Y; Babcock G; Cornelius J; Lamoreux ML; Boissy RE
Pigment Cell Res; 2000 Oct; 13(5):337-44. PubMed ID: 11041210
[TBL] [Abstract][Full Text] [Related]
3. Oculocutaneous albinism types 1 and 3 are ER retention diseases: mutation of tyrosinase or Tyrp1 can affect the processing of both mutant and wild-type proteins.
Toyofuku K; Wada I; Valencia JC; Kushimoto T; Ferrans VJ; Hearing VJ
FASEB J; 2001 Oct; 15(12):2149-61. PubMed ID: 11641241
[TBL] [Abstract][Full Text] [Related]
4. Tyrp1 Mutant Variants Associated with OCA3: Computational Characterization of Protein Stability and Ligand Binding.
Patel MH; Dolinska MB; Sergeev YV
Int J Mol Sci; 2021 Sep; 22(19):. PubMed ID: 34638544
[TBL] [Abstract][Full Text] [Related]
5. In vitro characterization of the intramelanosomal domain of human recombinant TYRP1 and its oculocutaneous albinism type 3-related mutant variants.
Dolinska MB; Anderson DE; Sergeev YV
Protein Sci; 2023 Jan; 32(1):e4518. PubMed ID: 36412553
[TBL] [Abstract][Full Text] [Related]
6. The etiology of oculocutaneous albinism (OCA) type II: the pink protein modulates the processing and transport of tyrosinase.
Toyofuku K; Valencia JC; Kushimoto T; Costin GE; Virador VM; Vieira WD; Ferrans VJ; Hearing VJ
Pigment Cell Res; 2002 Jun; 15(3):217-24. PubMed ID: 12028586
[TBL] [Abstract][Full Text] [Related]
7. Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4.
Costin GE; Valencia JC; Vieira WD; Lamoreux ML; Hearing VJ
J Cell Sci; 2003 Aug; 116(Pt 15):3203-12. PubMed ID: 12829739
[TBL] [Abstract][Full Text] [Related]
8. In silico screening and molecular dynamics simulation of disease-associated nsSNP in TYRP1 gene and its structural consequences in OCA3.
Kamaraj B; Purohit R
Biomed Res Int; 2013; 2013():697051. PubMed ID: 23862152
[TBL] [Abstract][Full Text] [Related]
9. The 5,6-dihydroxyindole-2-carboxylic acid (DHICA) oxidase activity of human tyrosinase.
Olivares C; Jiménez-Cervantes C; Lozano JA; Solano F; García-Borrón JC
Biochem J; 2001 Feb; 354(Pt 1):131-9. PubMed ID: 11171088
[TBL] [Abstract][Full Text] [Related]
10. Direct interaction of tyrosinase with Tyrp1 to form heterodimeric complexes in vivo.
Kobayashi T; Hearing VJ
J Cell Sci; 2007 Dec; 120(Pt 24):4261-8. PubMed ID: 18042623
[TBL] [Abstract][Full Text] [Related]
11. Minimal Efficacy of Nitisinone Treatment in a Novel Mouse Model of Oculocutaneous Albinism, Type 3.
Onojafe IF; Megan LH; Melch MG; Aderemi JO; Alur RP; Abu-Asab MS; Chan CC; Bernardini IM; Albert JS; Cogliati T; Adams DR; Brooks BP
Invest Ophthalmol Vis Sci; 2018 Oct; 59(12):4945-4952. PubMed ID: 30347088
[TBL] [Abstract][Full Text] [Related]
12. l-tyrosine induces melanocyte differentiation in novel pink-eyed dilution castaneus mouse mutant showing age-related pigmentation.
Hirobe T; Ishikawa A
J Dermatol Sci; 2015 Dec; 80(3):203-11. PubMed ID: 26475433
[TBL] [Abstract][Full Text] [Related]
13. Oculocutaneous albinism type 3: a Japanese girl with novel mutations in TYRP1 gene.
Yamada M; Sakai K; Hayashi M; Hozumi Y; Abe Y; Kawaguchi M; Ihn H; Suzuki T
J Dermatol Sci; 2011 Dec; 64(3):217-22. PubMed ID: 21996312
[TBL] [Abstract][Full Text] [Related]
14. Human tyrosinase related protein-1 (TRP-1) does not function as a DHICA oxidase activity in contrast to murine TRP-1.
Boissy RE; Sakai C; Zhao H; Kobayashi T; Hearing VJ
Exp Dermatol; 1998 Aug; 7(4):198-204. PubMed ID: 9758418
[TBL] [Abstract][Full Text] [Related]
15. Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".
Boissy RE; Zhao H; Oetting WS; Austin LM; Wildenberg SC; Boissy YL; Zhao Y; Sturm RA; Hearing VJ; King RA; Nordlund JJ
Am J Hum Genet; 1996 Jun; 58(6):1145-56. PubMed ID: 8651291
[TBL] [Abstract][Full Text] [Related]
16. Tyrosinase stabilization by Tyrp1 (the brown locus protein).
Kobayashi T; Imokawa G; Bennett DC; Hearing VJ
J Biol Chem; 1998 Nov; 273(48):31801-5. PubMed ID: 9822646
[TBL] [Abstract][Full Text] [Related]
17. Melanosomal defects in melanocytes from mice lacking expression of the pink-eyed dilution gene: correction by culture in the presence of excess tyrosine.
Rosemblat S; Sviderskaya EV; Easty DJ; Wilson A; Kwon BS; Bennett DC; Orlow SJ
Exp Cell Res; 1998 Mar; 239(2):344-52. PubMed ID: 9521852
[TBL] [Abstract][Full Text] [Related]
18. Biallelic mutations in L-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism.
Volk AE; Hedergott A; Preising M; Rading S; Fricke J; Herkenrath P; Nürnberg P; Altmüller J; von Ameln S; Lorenz B; Neugebauer A; Karsak M; Kubisch C
Hum Genet; 2021 Aug; 140(8):1157-1168. PubMed ID: 33959807
[TBL] [Abstract][Full Text] [Related]
19. Membrane transport proteins in melanosomes: Regulation of ions for pigmentation.
Wiriyasermkul P; Moriyama S; Nagamori S
Biochim Biophys Acta Biomembr; 2020 Dec; 1862(12):183318. PubMed ID: 32333855
[TBL] [Abstract][Full Text] [Related]
20. Mislocalization of melanosomal proteins in melanocytes from mice with oculocutaneous albinism type 2.
Manga P; Boissy RE; Pifko-Hirst S; Zhou BK; Orlow SJ
Exp Eye Res; 2001 Jun; 72(6):695-710. PubMed ID: 11384158
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]